[Effect of LAG3 deficiency on natural killer cell function and hepatic fibrosis in mice infected with ].

OBJECTIVE

To investigate the effect of LAG-3 deficiency (LAG3) on natural killer (NK) cell function and hepatic fibrosis in mice infected with .

METHODS

C57BL/6 mice, each weighing (20 ± 2) g, were divided into the LAG3 and wild type (WT) groups, and each mouse in both groups was inoculated with 3 000 protoscoleces via the hepatic portal vein. Mouse liver and spleen specimens were collected 12 weeks post-infection, sectioned and stained with sirius red, and the hepatic lesions and fibrosis were observed. Mouse hepatic and splenic lymphocytes were isolated, and flow cytometry was performed to detect the proportions of hepatic and splenic NK cells, the expression of CD44, CD25 and CD69 molecules on NK cell surface, and the secretion of interferon γ (IFN-γ), tumor necrosis factor α (TNF-α), interleukin (IL)-4, IL-10 and IL-17A.

RESULTS

Sirius red staining showed widening of inflammatory cell bands and hyperplasia of fibrotic connective tissues around mouse hepatic lesions, as well as increased deposition of collagen fibers in the LAG3-/-group relative to the WT group. Flow cytometry revealed lower proportions of mouse hepatic (6.29% ± 1.06% vs. 11.91% ± 1.85%, < 0.000 1) and splenic NK cells (4.44% ± 1.22% vs. 5.85% ± 1.10%, > 0.05) in the LAG3 group than in the WT group, and the mean fluorescence intensity of CD44 was higher on the surface of mouse hepatic NK cells in the LAG3 group than in the WT group ( = -3.234, < 0.01), while no significant differences were found in the mean fluorescence intensity of CD25 or CD69 on the surface of mouse hepaticNK cells between the LAG3 and WT groups (both values > 0.05). There were significant differences between the LAG3 and WT groups in terms of the percentages of IFN-γ ( = -0.723, > 0.05), TNF-α ( = -0.659, > 0.05), IL-4 ( = -0.263, > 0.05), IL-10 ( = -0.455, > 0.05) or IL-17A secreted by mouse hepatic NK cells ( = 0.091, > 0.05), and the percentage of IFN-γ secreted by mouse splenic NK cells was higher in the LAG3 group than in the WT group (58.40% ± 1.64% vs. 50.40% ± 4.13%; = -4.042, < 0.01); however, there were no significant differences between the two groups in terms of the proportions of TNF-α ( = -1.902, > 0.05), IL-4 ( = -1.333, > 0.05), IL-10 ( = -1.356, > 0.05) or IL-17A secreted by mouse splenic NK cells ( = 0.529, > 0.05).

CONCLUSIONS

During the course of infections, LAG3 promotes high-level secretion of IFN-γ by splenic NK cells, which may participate in the reversal the immune function of NK cells, resulting in aggravation of hepatic fibrosis.